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2,343 results for “Hydrachnidiae”
Fig. 1 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 1. Lebertia (Pilolebertia) porosa Thor, 1900 s. lat. A. Dorsal view. B. Ventral view showing acetabula. Photo: Reinhard Gerecke.
Fig. 2 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 2. Neighbor Joining tree based on COI barcodes of Norwegian specimens in the Lebertia porosa aggr. using the Kimura 2-Parameter substitution model. Bootstrap support (1000 replicates) above 70% is shown on branches.
Fig. 6 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 6. Lebertia (Pilolebertia) spp. Examples of observed differences in setation. A–B. High number of setae on segment five of legs three and four (III-L-5, IV-L-5) present in Lebertia aggr. spp. B and D. C. Gap in swimming setae on the fifth segment of the second leg (II-L-5) in Lebertia aggr. spp. A and B, and L. obscura Thor, 1900. D. Segment three of palp (P-3) with a double proximal long seta sometimes present in Lebertia aggr. spp. D. E–F. Segment five of the second leg (II-L-5), close-up: comparison of swimming setae with and without the large gap respectively.
Fig. 8 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 8. Lebertia (Pilolebertia) obscura Thor, 1900, ♂ from the type locality. A. Coxal field. B. Palp. C. I-L. D. II-L. E. III-L. F. IV-L. Scale bars = 100 µm.
Fig. 7 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 7. Lebertia (Pilolebertia) porosa Thor, 1900, ♂ from the type locality. A. Venter. B. Palp. C. I-L. D. II-L. E. III-L. F. IV-L. Scale bars = 100 µm.
Fig. 5 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 5. Lebertia (Pilolebertia) spp. from Norway. TCS haplotype network of COI sequences constructed with PopART.
Fig. 4 in Disentangling the identity of Lebertia porosa Thor, 1900 using integrative taxonomy (Acari: Hydrachnidia)
Fig. 4. Lebertia (Pilolebertia) spp. in Norway. Maximum Likelihood tree from analysis of the concatenated dataset (COI, 18S, 28S) in RAxML-NG. Bootstrap support (500 replicates) above 50% on branches.
Figure 4 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 4 Teutonia corsicanasp. nov., ♂ [CCDB 38559 F09], Ruisseau de Battesta, France: A – coxal and genital field, partial view; B – photograph of ejaculatory complex; C – palp, medial view; D – gnathosoma. Scale bars = 100 μm.
Figure 2 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 2 Results of ASAP analysis for COI sequences. (A) Distribution of pairwise differences, (B) Ranked pairwise differences.
Figure 1 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 1 Neighbour-Joining tree of the genusTeutonia, obtained from 17 nucleotide COI sequences.and the results of species delimitation analyses. Values near branches show bootstrap support (BS). The results of species delimitation by ASAP procedure are indicated by vertical bars. Country codes (alpha-2 code): DE – Germany, FR – France, MN – Montenegro, NO – Norway, TR – Turkey.
Figure 3 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 3 Teutonia corsicanasp. nov. (A-B, D-G – holotype ♀, Ruisseau de Tuara, France; C – ♀ [CCDB 38559 D12], preserved specimen, Riviere La Solenzara, France): A – coxal and genital field; B, C – genital field; D – palp, medial view (P-1 lacking); E – palp, lateral view; F – I-L-5 and -6; G – IV-L-5 and -6. Scale bars = 100 μm.
Figure 5 in A new water mite species of the genus Teutonia Koenike, 1889 from Corsica, France, based on morphological data and DNA barcodes (Acari, Hydrachnidia, Teutoniidae)
Figure 5 Teutonia cometes(Koch, 1837), ♀, Danilovgrad, spring under the bridge over the Zeta river, Montenegro: A – genital field; B – palp, medial view. Scale bar = 100 μm.
Figure 6 Collection sites. A in Water mites of the genusLebertia Neuman, 1880 from the eastern Himalayas (Acari: Hydrachnidia: Lebertiidae)
Figure 6 Collection sites. A – Haa River (Bhutan 03); B – Sertu Khola, Nunthala (Nepal 06); C – Garden stream, Nunthala (Nepal 05); D – Surke Khola (Nepal 04); E – stream S of Gokyo (Nepal 01); F – stream Dudh Kosi Nadi (Nepal 02). Authors: W. Klein (A), P.V. Veel (B-F).
Figure 3 in Water mites of the genusLebertia Neuman, 1880 from the eastern Himalayas (Acari: Hydrachnidia: Lebertiidae)
Figure 3 Lebertia(Lebertia) disparilisn. sp.., type series, ♂; A – coxal and genital field (partial view); B – right palp lateral; C – I-L-4-6; D – IV-L-4-6. Scale bars: 100 µm.
Figure 2 in Water mites of the genusLebertia Neuman, 1880 from the eastern Himalayas (Acari: Hydrachnidia: Lebertiidae)
Figure 2 Lebertia(Lebertia) khatriin. sp., type series. A-D, ♂; A – I-L-4-5; B – IV-L-4-6; C – right palp medial; D – coxal and genital field; E – ♀ genital. Scale bars: 100 µm.
Figure 1 in Water mites of the genusLebertia Neuman, 1880 from the eastern Himalayas (Acari: Hydrachnidia: Lebertiidae)
Figure 1 Lebertia(Lebertia) himalayaensisn. sp., type series. A-D, ♂; A – venter; B – gnathosoma with left palp and chelicera in situ; C – right palp medial; D – IV-L-3-6; E – ♀ genital field. Scale bars: 100 µm.
Figure 4 in Water mites of the genusLebertia Neuman, 1880 from the eastern Himalayas (Acari: Hydrachnidia: Lebertiidae)
Figure 4 Lebertia(Mixolebertia) veeli n. sp., type series. A-D, ♂; A – venter; B – IV-L-4-6; C – I-L-4-6; D – left palp medial; E – ♀ genital field. Scale bars: 100 µm.
Figure 2 in New records of water mites of the family Limnesiidae Thor from Australia (Acari: Hydrachnidia), with the description of seven new species
Figure 2 Limnesia (Limnesia) elongata sp. nov., holotype female. A – dorsum; B – venter; C – palp; D – IV – leg-4-6. Scale bars: A-B = 100
Figure 3 in New records of water mites of the family Limnesiidae Thor from Australia (Acari: Hydrachnidia), with the description of seven new species
Figure 3 Limnesia (Limnesia) gledhilli sp. nov., A-D – holotype male, E – paratype female. A – dorsum; B – venter; C – palp; D – IV-leg-5-6; E – venter. Scale bars: A-B, E = 200 µm, C-D =50 µm.
Figure 4 in Preliminary assessment of mating duration and prolonged post-copulatory associations in Arrenurus water mites (Actinotrichida: Parasitengonina: Hydrachnidiae)
Figure 4 Time spent on post-deposition behaviour (in %). Post-deposition behaviour is expressed as percentage of the total time spent on mating. The 25-75 percent quartiles are presented using a box. The medians are shown with a horizontal line inside the box. The minimal and maximal values are presented with the "whiskers". Petiolate species are indicated by light orange, and apetiolate ones by
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